Canonical Allele Identifier: CA317429754

Gene: KCNQ2

Linked Data

• ClinVar Variation Id: 495266
• ClinVar RCV Id: RCV000585831 ; RCV001306124 ; RCV002404589
• dbSNP Id: rs897976020
• gnomAD v2: 20-62045484-C-T
• gnomAD v4: 20-63414131-C-T
• MyVariant Identifiers: chr20:g.62045484C>T (hg19) ; chr20:g.63414131C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63414131C>T , CM000682.2:g.63414131C>T	GRCh38
NC_000020.10:g.62045484C>T , CM000682.1:g.62045484C>T	GRCh37
NC_000020.9:g.61515928C>T	NCBI36
NG_009004.1:g.63510G>A
NG_009004.2:g.63510G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1534G>A	ENSP00000516702.1:p.Glu512Lys
ENST00000359125.7:c.1588G>A MANE Select	ENSP00000352035.2:p.Glu530Lys
ENST00000637193.1:c.985G>A	ENSP00000490734.1:p.Glu329Lys
ENST00000344462.8:c.1495G>A	ENSP00000339611.4:p.Glu499Lys
ENST00000357249.6:c.1156G>A	ENSP00000349789.3:p.Glu386Lys
ENST00000359125.6:c.1588G>A	ENSP00000352035.2:p.Glu530Lys
ENST00000360480.7:c.1504G>A	ENSP00000353668.3:p.Glu502Lys
ENST00000370224.5:c.1504G>A	ENSP00000359244.2:p.Glu502Lys
ENST00000625514.2:c.1468G>A	ENSP00000486040.1:p.Glu490Lys
ENST00000626839.2:c.1534G>A	ENSP00000486706.1:p.Glu512Lys
ENST00000627221.2:c.645G>A
ENST00000629241.2:c.1504G>A	ENSP00000487142.1:p.Glu502Lys
ENST00000629318.1:c.196G>A	ENSP00000487384.1:p.Glu66Lys
ENST00000629676.2:c.1504G>A	ENSP00000486194.1:p.Glu502Lys
NM_004518.4:c.1504G>A	NP_004509.2:p.Glu502Lys
NM_172106.1:c.1534G>A	NP_742104.1:p.Glu512Lys
NM_172107.2:c.1588G>A	NP_742105.1:p.Glu530Lys
NM_172108.3:c.1495G>A	NP_742106.1:p.Glu499Lys
XM_006723787.1:c.1588G>A	XP_006723850.1:p.Glu530Lys
XM_011528807.1:c.1588G>A	XP_011527109.1:p.Glu530Lys
XM_011528808.1:c.1585G>A	XP_011527110.1:p.Glu529Lys
XM_011528809.1:c.1558G>A	XP_011527111.1:p.Glu520Lys
XM_011528810.1:c.1534G>A	XP_011527112.1:p.Glu512Lys
XM_011528811.1:c.1504G>A	XP_011527113.1:p.Glu502Lys
XM_011528812.1:c.1585G>A	XP_011527114.1:p.Glu529Lys
XM_011528813.1:c.1462G>A	XP_011527115.1:p.Glu488Lys
XM_011528814.1:c.1069G>A	XP_011527116.1:p.Glu357Lys
XM_011528815.1:c.1588G>A	XP_011527117.1:p.Glu530Lys
NM_004518.5:c.1504G>A	NP_004509.2:p.Glu502Lys
NM_172106.2:c.1534G>A	NP_742104.1:p.Glu512Lys
NM_172107.3:c.1588G>A	NP_742105.1:p.Glu530Lys
NM_172108.4:c.1495G>A	NP_742106.1:p.Glu499Lys
XM_011528810.2:c.1534G>A	XP_011527112.1:p.Glu512Lys
XM_011528811.2:c.1504G>A	XP_011527113.1:p.Glu502Lys
XM_017027841.2:c.1531G>A	XP_016883330.1:p.Glu511Lys
XM_017027842.2:c.1534G>A	XP_016883331.1:p.Glu512Lys
XM_017027843.1:c.1465G>A	XP_016883332.1:p.Glu489Lys
XM_017027844.2:c.1531G>A	XP_016883333.1:p.Glu511Lys
XM_017027845.1:c.496G>A	XP_016883334.1:p.Glu166Lys
NM_004518.6:c.1504G>A	NP_004509.2:p.Glu502Lys
NM_172106.3:c.1534G>A	NP_742104.1:p.Glu512Lys
NM_172107.4:c.1588G>A MANE Select	NP_742105.1:p.Glu530Lys
NM_172108.5:c.1495G>A	NP_742106.1:p.Glu499Lys
NM_001382235.1:c.1534G>A	NP_001369164.1:p.Glu512Lys